HsaINT0106866 @ hg38
Intron Retention
Gene
ENSG00000184956 | MUC6
Description
mucin 6, oligomeric mucus/gel-forming [Source:HGNC Symbol;Acc:HGNC:7517]
Coordinates
chr11:1023509-1024103:-
Coord C1 exon
chr11:1023947-1024103
Coord A exon
chr11:1023653-1023946
Coord C2 exon
chr11:1023509-1023652
Length
294 bp
Sequences
Splice sites
5' ss Seq
GCCGTGAGT
5' ss Score
8.56
3' ss Seq
GACAGCTCCCTTCCTCCCAGCCA
3' ss Score
5.07
Exon sequences
Seq C1 exon
GTATACCACCTGCCCTACTACGAGGCCTGCGTGCGCGACGCATGTGGGTGTGACAGTGGCGGGGACTGTGAGTGTCTGTGCGATGCCGTGGCTGCCTACGCCCAAGCCTGTCTGGACAAGGGTGTGTGCGTGGACTGGAGGACCCCGGCCTTCTGCC
Seq A exon
GTGAGTGACCACCCCTCCCACAGGTTGCTCCAGCCCCTGCCACCCAGCGCCACTAAGGGCCGGCGCAGGGCTGCCCTTGCCCACAGGCCCCTCTCCCTGGACAGGCGCCGGGCTGTGCCCTGCGGGGCCACCCTGGCCCTCCCGCAGCCCCCAGCTGCCCAGGGGAGGCTTCACCAAGAGGGCCCAGACCTTCCCCGCCCACACTCAGGTTCCATGCATGCCCAGGGGAACCACCGGGTCAGGGCCAGGGCCAGGGCCAGGAACCCCACCAGCTGACAGCTCCCTTCCTCCCAG
Seq C2 exon
CCATCTACTGCGGCTTCTACAACACGCACACGCAGGACGGCCATGGCGAGTACCAGTACACACAGGAGGCCAACTGCACGTGGCACTACCAGCCCTGCCTCTGCCCCAGCCAGCCACAGAGCGTCCCAGGCAGCAACATCGAAG
VastDB Features
Vast-tools module Information
Secondary ID
ENSG00000184956:ENST00000421673:25
Average complexity
IR
Mappability confidence:
NA
Protein Impact
ORF disruption upon sequence inclusion
No structure available
Features
Disorder rate (Iupred):
C1=0.000 A=NA C2=0.000
Domain overlap (PFAM):
C1:
PF087426=C8=FE(69.3=100)
A:
NA
C2:
PF087426=C8=PD(0.1=0.0)
Main Inclusion Isoform:
NA
Other Inclusion Isoforms:
NA
Other Skipping Isoforms:
NA
Associated events
Other assemblies
Conservation
Fruitfly
(dm6)
No conservation detected
Primers PCR
Suggestions for RT-PCR validation
F:
TACCACCTGCCCTACTACGAG
R:
CTTCGATGTTGCTGCCTGGG
Band lengths:
298-592
Functional annotations
There are 0 annotated functions for this event
GENOMIC CONTEXT[edit]
INCLUSION PATTERN[edit]
SPECIAL DATASETS
- Genotype-Tissue Expression Project (GTEx)
- Autistic and control brains
- Pre-implantation embryo development